Clearance Summary
CODENT LOW SPEED DENTAL HANDPIECES AND ACCESSORIES received FDA 510(k) clearance under submission number K133069, sponsored by Codent Technical Industry Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2014-10-24.
- Submission: K133069
- Applicant / Sponsor: Codent Technical Industry Co., Ltd.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class I
- Regulation citation: 21 CFR 872.4200
- Decision date: 2014-10-24
Classification & Regulation
This clearance is catalogued under FDA product code EFB and 21 CFR 872.4200, within the Dental review panel as a Class I device.